Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Disease and BMP2[original query] |
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| Polymorphism of VDR gene--the most effective molecular marker of osteoporotic bone fractures risk within postmenopausal women from Wielkopolska region of Poland. Endokrynologia Polska 0 56 (3): 233-9. Horst-Sikorska Wanda, Wawrzyniak Anna, Celczy?ska-Bajew Liliana, Marcinkowska Michalina, Dabrowski Sebastian, Kalak Robert, S?omski Rysza |
| Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance. American journal of human genetics 2007 Oct 81 (4): 799-807. Milet Jacqueline, Dehais Valerie, Bourgain Catherine, Jouanolle Anne Marie, Mosser Annick, Perrin Michele, Morcet Jeff, Brissot Pierre, David Veronique, Deugnier Yves, Mosser Je |
| Investigation of the association of BMP gene variants with nephropathy in Type 1 diabetes mellitus. Diabetic medicine : a journal of the British Diabetic Association 2010 Jun 27 (6): 624-30. McKnight A J, Pettigrew K A, Patterson C C, Kilner J, Sadlier D M, Maxwell A P, |
| Evaluation of germline BMP4 mutation as a cause of colorectal cancer. Human mutation 2011 Jan 32 (1): E1928-38. Lubbe Steven J, Pittman Alan M, Matijssen Cornelis, Twiss Philip, Olver Bianca, Lloyd Amy, Qureshi Mobshra, Brown Nathan, Nye Emma, Stamp Gordon, Blagg Julian, Houlston Richard |
| Identification of genes for bone mineral density variation by computational disease gene identification strategy. Journal of bone and mineral metabolism 2011 Nov 29 (6): 709-16. Li Gloria H Y, Deng Hong-Wen, Kung Annie W C, Huang Qing-Ya |
| Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. PLoS genetics 2011 Jun 7 (6): e1002105. Tomlinson Ian P M, Carvajal-Carmona Luis G, Dobbins Sara E, Tenesa Albert, Jones Angela M, Howarth Kimberley, Palles Claire, Broderick Peter, Jaeger Emma E M, Farrington Susan, Lewis Annabelle, Prendergast James G D, Pittman Alan M, Theodoratou Evropi, Olver Bianca, Walker Marion, Penegar Steven, Barclay Ella, Whiffin Nicola, Martin Lynn, Ballereau Stephane, Lloyd Amy, Gorman Maggie, Lubbe Steven, , , , Howie Bryan, Marchini Jonathan, Ruiz-Ponte Clara, Fernandez-Rozadilla Ceres, Castells Antoni, Carracedo Angel, Castellvi-Bel Sergi, Duggan David, Conti David, Cazier Jean-Baptiste, Campbell Harry, Sieber Oliver, Lipton Lara, Gibbs Peter, Martin Nicholas G, Montgomery Grant W, Young Joanne, Baird Paul N, Gallinger Steven, Newcomb Polly, Hopper John, Jenkins Mark A, Aaltonen Lauri A, Kerr David J, Cheadle Jeremy, Pharoah Paul, Casey Graham, Houlston Richard S, Dunlop Malcolm |
| Genetic variation in the transforming growth factor-ß signaling pathway and survival after diagnosis with colon and rectal cancer. Cancer 2011 Sep 117 (18): 4175-83. Slattery Martha L, Lundgreen Abbie, Herrick Jennifer S, Wolff Roger K, Caan Bette |
| Association of Caucasian-identified variants with colorectal cancer risk in Singapore Chinese. PloS one 2012 7 (8): e42407. Thean Lai Fun, Li Hui Hua, Teo Yik Ying, Koh Woon-Puay, Yuan Jian-Min, Teoh Mei Lin, Koh Poh Koon, Tang Choong Leong, Cheah Peh Ye |
| Genetic association analysis in a clinically and histologically confirmed otosclerosis population confirms association with the TGFB1 gene but suggests an association of the RELN gene with a clinically indistinguishable otosclerosis-like phenotype. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2014 Jul 35 (6): 1058-64. Sommen Manou, Van Camp Guy, Liktor Balázs, Csomor Péter, Fransen Erik, Sziklai István, Schrauwen Isabelle, Karosi Tam |
| Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes. Blood cells, molecules & diseases 2015 Jun 55 (1): 71-5. Radio Francesca Clementina, Majore Silvia, Aurizi Caterina, Sorge Fiammetta, Biolcati Gianfranco, Bernabini Sara, Giotti Irene, Torricelli Francesca, Giannarelli Diana, De Bernardo Carmelilia, Grammatico Pao |
| [Polymorphism of bone morphogenetic protein (BMP2) and osteoporosis etiology]. Ginekologia polska 2015 Mar 86 (3): 203-9. Wolski Hubert, Bogacz Anna, Bartkowiak-Wieczorek Joanna, Greber Agnieszka, Pie?kowski Wojciech, Drews Krzysztof, Klejewski Andrzej, Seremak-Mrozikiewicz Agniesz |
| Unveiling the interactions among BMPR-2, ALK-1 and 5-HTT genes in the pathophysiology of HAPE. Gene 2016 May . Ali Zahara, Waseem Mohammad, Kumar Rahul, Pandey Priyanka, Mohammad Ghulam, Qadar Pasha M |
| Genotypic and phenotypic predictors of inflammation in patients with chronic kidney disease. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2016 Apr . Luttropp Karin, Debowska Malgorzata, Lukaszuk Tomasz, Bobrowski Leon, Carrero Juan Jesus, Qureshi Abdul Rashid, Stenvinkel Peter, Lindholm Bengt, Waniewski Jacek, Nordfors Loui |
Genetic Variants in the Bone Morphogenic Protein Gene Family Modify the Association between Residential Exposure to Traffic and Peripheral Arterial Disease.
PloS one 2016 11 (4): e0152670. Ward-Caviness Cavin K, Neas Lucas M, Blach Colette, Haynes Carol S, LaRocque-Abramson Karen, Grass Elizabeth, Dowdy Elaine, Devlin Robert B, Diaz-Sanchez David, Cascio Wayne E, Lynn Miranda Marie, Gregory Simon G, Shah Svati H, Kraus William E, Hauser Elizabeth |
| De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis. Proceedings of the National Academy of Sciences of the United States of America 2017 8 114 (35): E7341-E7347. Timberlake Andrew T, Furey Charuta G, Choi Jungmin, Nelson-Williams Carol, , Loring Erin, Galm Amy, Kahle Kristopher T, Steinbacher Derek M, Larysz Dawid, Persing John A, Lifton Richard |
| Functional polymorphisms in asporin and CILP together with joint loading predispose to hand osteoarthritis. BMC genetics 2017 Dec 18 (1): 108. Taipale Mari, Solovieva Svetlana, Leino-Arjas Päivi, Männikkö Min |
| Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population. Human genetics 2018 May . Mowat Andrew J, Crompton Michael, Ziff Joanna L, Aldren Christopher P, Lavy Jeremy A, Saeed Shakeel R, Dawson Sally |
| Nomograms incorporating genetic variants in BMP/Smad4/Hamp pathway to predict disease outcomes after definitive radiotherapy for non-small cell lung cancer. Cancer medicine 2018 May . Yang Ju, Xu Ting, Gomez Daniel R, Yuan Xianglin, Nguyen Quynh-Nhu, Jeter Melenda, Song Yipeng, Komaki Ritsuko, Hu Ye, Hahn Stephen M, Liao Zhongxi |
| Bone mineral density and the 570A>T polymorphism of the bone morphogenetic protein 2 (BMP2) gene in patients with inflammatory bowel disease: a cross-sectional study. Journal of physiology and pharmacology : an official journal of the Polish Physiological Society 2017 Oct 68 (5): 757-764. Krela-Kazmierczak I, Wawrzyniak A, Szymczak A, Eder P, Lykowska-Szuber L, Michalak M, Drweska-Matelska N, Kaczmarek-Rys M, Skrzypczak-Zielinska M, Szalata M, Slomski |
| Common Genetic Variants on Bone Morphogenetic Protein Receptor Type IB (BMPR1B) Gene Are Predictive for Carotid Intima-Media Thickness. Circulation journal : official journal of the Japanese Circulation Society 2019 2 83 (4): 749-756. Wu Yih-Jer, Lee Yi-Nan, Wu Tzu-Wei, Chou Chao-Liang, Wang Li- |
| Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry.
The pharmacogenomics journal 2019 Dec . de Las Fuentes L, Sung Y J, Sitlani C M, Avery C L, Bartz T M, Keyser C de, Evans D S, Li X, Musani S K, Ruiter R, Smith A V, Sun F, Trompet S, Xu H, Arnett D K, Bis J C, Broeckel U, Busch E L, Chen Y-D I, Correa A, Cummings S R, Floyd J S, Ford I, Guo X, Harris T B, Ikram M A, Lange L, Launer L J, Reiner A P, Schwander K, Smith N L, Sotoodehnia N, Stewart J D, Stott D J, Stürmer T, Taylor K D, Uitterlinden A, Vasan R S, Wiggins K L, Cupples L A, Gudnason V, Heckbert S R, Jukema J W, Liu Y, Psaty B M, Rao D C, Rotter J I, Stricker B, Wilson J G, Whitsel E |
| Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders. The Journal of clinical endocrinology and metabolism 2021 Mar . Vishnopolska Sebastian Alexis, Mercogliano Maria Florencia, Camilletti Maria Andrea, Mortensen Amanda Helen, Braslavsky Debora, Keselman Ana, Bergadá Ignacio, Olivieri Federico, Miranda Lucas, Marino Roxana, Ramírez Pablo, Pérez Garrido Natalia, Patiño Mejia Helen, Ciaccio Marta, Di Palma Maria Isabel, Belgorosky Alicia, Martí Marcelo Adrian, Kitzman Jacob Otto, Camper Sally Ann, Pérez-Millán Maria In |
| Investigation of the Role of BMP2 and -4 in ASD, VSD and Complex Congenital Heart Disease. Diagnostics (Basel, Switzerland) 2023 8 13 (16): . Dimitrios Bobos, Giannoula Soufla, Dimitrios C Angouras, Ioannis Lekakis, Sotirios Georgopoulos, Euthemia Melissa |
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